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PROSPECTIVE RANDOMISED CONTROLLED TRIAL TO SEE THE FEASIBILITY AND SAFETY OF TROPHIC FEED IN PATIENTS OF HAEMORRHAGIC SHOCK

PROSPECTIVE RANDOMISED CONTROL TRIAL TO ASSESS THE FEASIBILITY AND SAFETY OF TROPHIC FEED IN PATIENTS WITH HAEMORRHAGIC SHOCK ADMITTED IN TRAUMA CARE ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028406
Enrollment
50
Registered
2020-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: T794- Traumatic shock

Interventions

Intervention1: Trophic Feed: Group A will include 25 patients with shock with or without inotropes getting trophic feed within 24 hrs of admission in ICU. Group B will include 25 patients with shock w

Sponsors

AIIMS NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients admitted with haemorrhagic shock in trauma care ICU will be included in study

Exclusion criteria

Exclusion criteria: 1.Bowel obstruction 2.Protracted ileus 3.Intractable vomiting 4.Major upper gastrointestinal bleed 5.Patient underwent any bowel surgery

Design outcomes

Primary

MeasureTime frame
Primary outcome will be to see the tolerability of trophic feed.Timepoint: 1ST, 2ND, 3RD, 4TH, 5TH DAY—

Secondary

MeasureTime frame
1.Incidence of VAP 2.Incidence of CLABSI 3.Length of mechanical ventilation 4.Length of ionotrophic support 5.Duration of ICU stay Timepoint: 1ST, 2ND, 3RD, 4TH, 5TH DAY—

Countries

India

Contacts

Public Contactshrikant

AIIMS, New Delhi

amitguptaaiims@gmail.com9999882283

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026